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蕈样肉芽肿/赛泽里综合征的生存结局和预后因素:修订的国际皮肤淋巴瘤学会/欧洲癌症研究与治疗组织分期建议的验证。

Survival outcomes and prognostic factors in mycosis fungoides/Sézary syndrome: validation of the revised International Society for Cutaneous Lymphomas/European Organisation for Research and Treatment of Cancer staging proposal.

机构信息

Guy's and St Thomas' National Health Service (NHS) Foundation Trust, London, United Kingdom.

出版信息

J Clin Oncol. 2010 Nov 1;28(31):4730-9. doi: 10.1200/JCO.2009.27.7665. Epub 2010 Sep 20.

Abstract

PURPOSE

We have analyzed the outcome of mycosis fungoides (MF) and Sézary syndrome (SS) patients using the recent International Society for Cutaneous Lymphomas (ISCL)/European Organisation for Research and Treatment of Cancer (EORTC) revised staging proposal.

PATIENTS AND METHODS

Overall survival (OS), disease-specific survival (DSS), and risk of disease progression (RDP) were calculated for a cohort of 1,502 patients using univariate and multivariate models.

RESULTS

The mean age at diagnosis was 54 years, and 71% of patients presented with early-stage disease. Disease progression occurred in 34%, and 26% of patients died due to MF/SS. A significant difference in survival and progression was noted for patients with early-stage disease having patches alone (T1a/T2a) compared with those having patches and plaques (T1b/T2b). Univariate analysis established that (1) advanced skin and overall clinical stage, increased age, male sex, increased lactate dehydrogenase (LDH), and large-cell transformation were associated with reduced survival and increased RDP; (2) hypopigmented MF, MF with lymphomatoid papulosis, and poikilodermatous MF were associated with improved survival and reduced RDP; and (3) folliculotropic MF was associated with an increased RDP. Multivariate analysis established that (1) advanced skin (T) stage, the presence in peripheral blood of the tumor clone without Sézary cells (B0b), increased LDH, and folliculotropic MF were independent predictors of poor survival and increased RDP; (2) large-cell transformation and tumor distribution were independent predictors of increased RDP only; and (3) N, M, and B stages; age; male sex; and poikilodermatous MF were only significant for survival.

CONCLUSION

This study has validated the recently proposed ISCL/EORTC staging system and identified new prognostic factors.

摘要

目的

我们使用最近的国际皮肤淋巴瘤学会(ISCL)/欧洲癌症研究与治疗组织(EORTC)修订的分期建议,分析蕈样肉芽肿(MF)和 Sézary 综合征(SS)患者的结局。

患者和方法

使用单变量和多变量模型,对 1502 例患者队列的总生存(OS)、疾病特异性生存(DSS)和疾病进展风险(RDP)进行了计算。

结果

诊断时的平均年龄为 54 岁,71%的患者处于早期疾病阶段。34%的患者出现疾病进展,26%的患者死于 MF/SS。仅有斑块(T1a/T2a)的早期疾病患者与既有斑块又有斑块的患者(T1b/T2b)相比,生存和进展差异显著。单变量分析确定:(1)晚期皮肤和总体临床分期、年龄增加、男性、乳酸脱氢酶(LDH)升高和大细胞转化与生存率降低和 RDP 增加相关;(2)色素减退 MF、伴淋巴瘤样丘疹病的 MF 和斑驳性 MF 与生存改善和 RDP 降低相关;(3)滤泡性 MF 与 RDP 增加相关。多变量分析确定:(1)晚期皮肤(T)分期、外周血中存在无 Sézary 细胞的肿瘤克隆(B0b)、LDH 升高和滤泡性 MF 是生存率降低和 RDP 增加的独立预测因素;(2)大细胞转化和肿瘤分布仅为 RDP 增加的独立预测因素;(3)N、M 和 B 期;年龄;男性;以及斑驳性 MF 仅对生存有意义。

结论

本研究验证了最近提出的 ISCL/EORTC 分期系统,并确定了新的预后因素。

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